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FIGURE 1 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 1 | Partial sequence of nucleotides and amino acids (AA) encoding glut2 (glucose transporter 2) from Petenia splendida taken from Gen Bank to design specific oligonucleotides for qPCR.
FIGURE 3 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 3 | Phylogenetic tree based on the sequence of glut2 (glucose transporter 2) from Petenia splendida and other teleosts using the neighbor-joining (NJ) method. Values at branch points represent percentage frequencies for tree topology after 1,000 interations.
FIGURE 4 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 4 | Relative expression of glut2 in kidney (K), liver (L), muscle (M), brain (B), pancreas (P), gill (G), heart (H), intestine (I), stomach (S) and testis (T) of adult Petenia splendida (mean ± SEM; n = 3). Lowercase letters indicate significant differences between the expression level in the tissues (p <0.05).
FIGURE 2 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 2 | Amino acid sequence of glut2 in Petenia splendida aligned with other species other species of teleost fish. Identical amino acids are presented in black, and the high and less conserved amino acids are presented in gray and period, respectively.
FIGURE 5 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 5 | Relative expression of glut2 during the early ontogeny of Petenia splendida. Lowercase letters indicate significant differences in the expression of glut2 as a function of developmental time (p <0.05). AN: Artemia nauplii (3–10 dph), CF: cofeeding (Artemia nauplii and tilapia feed) (11–13 dph), TF: trout feed (14–30 dph) (mean ± SEM; n = 3).
FIGURE 3 in Molecular characterization of Astyanax species (Characiformes: Characidae) from the upper Paraguaçu River basin, a hydrographic system with high endemism
FIGURE 3 | Species tree showing phylogenetic relationships for Astyanax's MOTUs from the upper Paraguaçu River basin. The tree was generated using approximately 2,230 bp obtained for the COI, Cytb, and S7 sequences for the samples indicated in Tab. S1. The topology corresponds to the Bayesian tree. The numbers on the branches are bootstrap values for the posterior probability for Bayesian species tree and speciation probability values of BP&P species delimitation. The scale bar indicates nucleotide substitutions per site.
FIGURE 2 in Molecular characterization of Astyanax species (Characiformes: Characidae) from the upper Paraguaçu River basin, a hydrographic system with high endemism
FIGURE 2 | Bayesian tree showing phylogenetic relationships among Astyanax species, using 1,792 COI sequences available in the Bold system database, and 75 ones produced in this study for specimens of Astyanax endemic to the upper Paraguaçu River basin. A. Clusters (black) for the clade 1 formed by Astyanax species closely related to the specimens collected in the Paraguaçu River; and clusters (grey) for the remaining analyzed Astyanax species. B. Clade 1 in details, depicting the delimitation species results using BIN, ABGD, and GMYC approaches. Black rectangles represent the distinct number of MOTUs identified by the three analyses: BIN (MOTU 1-5); ABGD (MOTU 1-19); GMYC (MOTU 1-50). The numbers in the nodes correspond to the main clusters of species (Tab. S2). Nodes marked with an asterisk denote posterior probabilities greater than 0.9. Species of Astyanax from the upper Paraguaçu River basin are highlighted in colored rectangles. Astyanax sp. sequences were download from BOLD system database. Our studied species are in bold letters. The colors of the species name are highlighted in accordance with Fig. 1.
FIGURE 1 in Molecular characterization of Astyanax species (Characiformes: Characidae) from the upper Paraguaçu River basin, a hydrographic system with high endemism
FIGURE 1 | Map of the Paraguaçu River basin, Bahia, northeastern Brazil, showing collection sites of Astyanax species sampled in this study and for two Astyanax sp. available in the BOLD system database (*), with the exception of A. hamatilis. Astyanax rupestris from the Coisa Boa River (dark blue square) and Cumbuca River (dark blue circle), A. aff. rupestris from the Piabinha River (half yellow and blue circle), Astyanax sp. from the Piabinha River (orange circle*), A. lorien from the Preto River (pink circle), Astyanax sp. from Coité River (brown circle*), A. brucutu from the Pratinha River (red circle), and A. epiagos from the Ferro Doido River (green circle). The colors of the symbols on the map are in accordance with Fig. 2. Scale 1:1300723.
Figure 11 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 11. The efficacy of RM of orange peels against human pathogenic bacteria. ****Extremely significant among compared groups at p <0.05 level. Test 1: RM of Valen-cia orange; Test 2: RM of Mandarin orange; Test 3: RM of African navel orange.
Figure 6 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 6. The structure of bioactive compounds of RM of African Navel orange peel (1) Limonene; (2) Hexadecanoic acid, 2-hydroxy-1- (hydroxymethyl) ethyl; (3) 9,12-Octadecadienoic acid (Z,Z)-, methyl ester; (4) Terephthalic acid, di(2-ethylhexyl) ester; (5) α-Sitosterol; (6) α-D-Glucopyranose, 4-O-α-D-galactopyranosyl-; (7) 2-Methoxy-4-vinylphenol; (8) Eugenol; (9) cis-Vaccenic acid; (10) De-canal; (11) Vitamin E; (12) Dichloroxylenol.
Figure 3 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 3. GC-MS chromatogram of the RMs of orange peels. (A) RM of Valencia orange; (B) RM of Mandarin orange; (C) RM of African Navel orange.
Figure 2 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 2. The morphology of orange fruits. (A) Valenica orange; (B) Madarin orange; (C) African Navel orange.
Figure 4 in Isolation and characterization of Klebsiella oxytoca from the rhizosphere of Lotus corniculatus and its biostimulating features
Figure 4. Enhancement of the root and shoot lengths of barley when inoculated with LCK121. *Indicates a significant effect (P value <0.05).
Figure 1 in Molecular characterization of Giardia lamblia and risk factors for giardiasis among immunocompromised patients in southern Brazil
Figure 1. Similarity between sequences of the gdh gene of isolates from G. lamblia in immunocompromised patients in southern Brazil (P01 to P18) and sequences of the parasite found in Brazil and stored in the GenBank, by the Neighbor-Joining (NJ) method with 1000-replicate bootstrap (A) and by the Maximum Likelihood (ML) method with 1000-replicate bootstrap (B). Bootstrap values below 50 were omitted.
Figure 5 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 5. The structure of bioactive compounds of RM of Mandarin orange peel (1) Lim-onene; (2) Octadecanoic acid, 2-hydroxy-1- (hydroxymethyl) ethyl; (3) Hexadecanoic acid, 2-hydroxy-1-(hydroxymethyl) ethyl; (4) Tetradecanamide; (5) n-Hexadecanoic acid; (6) α-D-Mannofuranoside, 1-O-(10-undecenyl)-; (7) 3-Deoxy-d-mannoic lactone; (8) Desulpho-sinigrin; (9) 2-Methoxy-4-vinylphenol; (10) Decanal; (11) Vitamin E; (12) 1-Monolinoleoylglycerol trimethylsilyl ether.
Figure 3 in Isolation and characterization of Klebsiella oxytoca from the rhizosphere of Lotus corniculatus and its biostimulating features
Figure 3. Enhancement of the root and shoot lengths of barley when inoculated with LCK121, A.LCK121-treated ones; B.control seedlings.
Figure 2 in Molecular characterization of Giardia lamblia and risk factors for giardiasis among immunocompromised patients in southern Brazil
Figure 2. Similarity between sequences of the gdh gene of isolates from G. lamblia in immunocompromised patients in southern Brazil (P01 to P18) and sequences of the parasite in different countries and stored in the GenBank, by the Neighbor-Joining (NJ) method with 1000-replicate bootstrap (A) and by the Maximum Likelihood (ML) method with 1000-replicate bootstrap (B). Bootstrap values below 50 were omitted.
Figure 2 in Isolation and characterization of Klebsiella oxytoca from the rhizosphere of Lotus corniculatus and its biostimulating features
Figure 2. Evolutionary relationships of LCK121 and other related bacterial species as inferred using the neighbor-joining method.
Figure 5 in Isolation and characterization of Klebsiella oxytoca from the rhizosphere of Lotus corniculatus and its biostimulating features
Figure 5. Enhancement of the root and shoot dry weight of barley when inoculated with LCK121. *Indicates a significant effect (P value <0.05).
Figure 4 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 4. The structure of bioactive compounds of RM of Valencia orange peel (1) Limonene; (2) 9-Octadecenamide, (Z)-; (3) Hexadecanoic acid, 2- hy-droxy-1-(hydroxymethyl)ethyl; (4) Octadecanoic acid, 2-hydroxy-1-(hydroxymethyl)ethyl; (5) Tetradecanamide; (6) Hexadecanamide; (7) Ethyl iso-allocholate; (8) Ethyl α-d-glucopyranoside; (9) d-Glycero-d-galacto-heptose; (10) α-Sitosterol; (11) Vitamin E; (12) 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.